Examining the Most Effective Method to Reduce Running Ground Contact Time
2 other identifiers
interventional
30
1 country
1
Brief Summary
The purpose of our study is to establish the most effective running retraining technique to decrease ground contact time. This will be investigated by applying three running retraining conditions and assessing the change in ground contact time and other biomechanical variables between the runner's baseline running and each retraining technique.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 18, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedFirst Posted
Study publicly available on registry
May 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
December 12, 2025
December 1, 2025
1.6 years
April 18, 2025
December 5, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Ground Contact Time
The amount of time in milliseconds that the foot remains in contact with the ground while running. GCT will be measured through the RunScribe device.
Within a single session, measured pre-intervention (baseline) and during each running condition intervention
Secondary Outcomes (4)
Step Rate
Within a single session, measured pre-intervention (baseline) and during each running condition intervention
Average Vertical Loading Rate (AVLR)
Within a single session, measured pre-intervention (baseline) and during each running condition intervention
Braking Impulse
Within a single session, measured pre-intervention (baseline) and during each running condition intervention
Step Length
Within a single session, measured pre-intervention (baseline) and during each running condition intervention
Study Arms (1)
Run Retraining Conditions
EXPERIMENTALSingle-arm, within subject, repeated measures design. All participants will run at baseline and then under 3 different running conditions.
Interventions
Runners will be instructed to match their step rate to a target step rate, 10% above their baseline step rate. A metronome will be played over a speaker to provide real-time auditory feedback of the target step rate.
The clinician will provide real-time verbal feedback to runner to "pull your foot off the ground as quickly as you can," every 15 seconds during the retraining condition.
Runners will visualize their real-time ground contact time (GCT) measured by the RunScribe on a TV screen. They will be instructed to run with a goal of matching their target GCT. Their target GCT will be 5% less than their baseline.
Eligibility Criteria
You may qualify if:
- Military Service Member or USMA cadet between the ages of 17-60
- Run at least 2 miles three times per week for the past 3 months
- Able to run for at least 15 continuous minutes at a self-selected speed
- Fluent in the English language to read and provide informed consent and follow study instructions
You may not qualify if:
- Lower extremity or low back pain in the previous 3 months
- Lower extremity or low back surgery in the previous 6 months
- Self-reported pregnancy or given birth within the last 6 months
- Currently on a profile that restricts or limits running
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Keller Army Community Hospital
West Point, New York, 10996, United States
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- FED
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 18, 2025
First Posted
May 25, 2025
Study Start
May 1, 2025
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
December 12, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share
We do not have a data sharing agreement or plan to share IDP as part of our IRB protocol.